首页 | 本学科首页   官方微博 | 高级检索  
     


Neuropeptide Y5 receptor antagonism does not induce clinically meaningful weight loss in overweight and obese adults
Authors:Erondu Ngozi  Gantz Ira  Musser Bret  Suryawanshi Shailaja  Mallick Madhuja  Addy Carol  Cote Josee  Bray George  Fujioka Ken  Bays Harold  Hollander Priscilla  Sanabria-Bohórquez Sandra M  Eng WaiSi  Långström Bengt  Hargreaves Richard J  Burns H Donald  Kanatani Akio  Fukami Takehiro  MacNeil Douglas J  Gottesdiener Keith M  Amatruda John M  Kaufman Keith D  Heymsfield Steven B
Affiliation:Merck & Co., Inc., 126 E. Lincoln Avenue, Rahway, New Jersey 07065.
Abstract:Neuropeptide Y (NPY) is a potent orexigenic neuropeptide, and antagonism of NPY Y1 and NPY Y5 receptors (NPYxR) is considered a potentially important anti-obesity drug target. We tested the hypothesis that blockade of the NPY5R will lead to weight loss in humans using MK-0557, a potent, highly selective, orally active NPY5R antagonist. The initial series of experiments reported herein, including a multiple-dose positron-emission tomography study and a 12 week proof-of concept/dose-ranging study, suggested an optimal MK-0557 dose of 1 mg/day. The hypothesis was then tested in a 52 week, multicenter, randomized, double-blind, placebo-controlled trial involving 1661 overweight and obese patients. Although statistically significant at 52 weeks, the magnitude of induced weight loss was not clinically meaningful. These observations provide the first clinical insight into the human NPY-energy homeostatic pathway and suggest that solely targeting the NPY5R in future drug development programs is unlikely to produce therapeutic efficacy.
Keywords:MOLNEURO   HUMDISEASE   CHEMBIO
本文献已被 ScienceDirect PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号